Phenytoin Suspension
Product Images NDC 51672-4069

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Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Phenytoin (NDC 51672-4069). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sun Pharmaceutical Industries, Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Chemical Structure (Phenytoin 01)

FDA Label Image

Principal Display Panel (237 mL Bottle Label)

Principal Display Panel (237 mL Bottle Label)
This is a medication with NDC code 51672-4069-1. It contains Phenytoin in a 5 mL dose of 125 mg. It comes with a Medication Guide and the recommended dosage for adults is one teaspoonful three times a day. The package insert should be consulted for pediatric patients' dosages. Patients are advised to be informed of the dosing schedule by their pharmacists. The medication should be stored at 20° to 25°C [68° to 77°F] and away from children. It is manufactured by Taro Pharmaceutical Industries Ltd. located in Haifa Bay, Israel. It is distributed in the U.S. by Taro Pharmaceuticals U.S.A., Inc. The medication should be shaken well before use and should not be used for parenteral administration.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.